DUPLICATION OF LEADER SEQUENCE FOR PROTEIN TARGETING TO MITOCHONDRIA LEADS TO INCREASED IMPORT EFFICIENCY

被引:43
作者
GALANIS, M
DEVENISH, RJ
NAGLEY, P
机构
[1] MONASH UNIV,DEPT BIOCHEM,CLAYTON,VIC 3168,AUSTRALIA
[2] MONASH UNIV,CTR MOLEC BIOL & MED,CLAYTON,VIC 3168,AUSTRALIA
关键词
MITOCHONDRIAL ATPASE COMPLEX; CHIMERIC FUSION PROTEIN; INTEGRAL MEMBRANE PROTEIN; LEADER PEPTIDE; PROTEIN IMPORT; SACCHAROMYCES-CEREVISIAE;
D O I
10.1016/0014-5793(91)80529-C
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We describe a novel method for enhancing protein import into mitochondria, by tandemyl duplicating the N-terminal cleavable leader peptide using a gene manipulation strategy. The import into isolate yeast mitochondria of passenger proteins (yeast mitochondrial ATP synthase subunits 8 and 9 and some mutagenised derivatives) that show little or no import when endowed with one such leader (that of Neurospora crassa mitochondrial ATP synthase subunit 9) is remarkably improved when the leader is tandemly duplicated. The import of these chimaeric proteins bearing a double leader is so rapid that a series of partially processed precursor intermediates accumulates inside the mitochondria before the final proteolytic release of leader sequences from the passenger proteins. It is considered that the duplicated leader greatly accelerates delivery of the import precursors to outer membrane receptor elements and the associated translocation systems, thereby enhancing precursor uptake into mitochondria.
引用
收藏
页码:425 / 430
页数:6
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